Synthesis and enantiomeric recognition studies of optically active 5,5-dioxophenothiazine bis(urea) and bis(thiourea) derivatives

Dávid Pál, Ildikó Móczár, Attila Kormos, P. Baranyai, P. Huszthy

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Novel optically active 5,5-dioxophenothiazine bis(urea) and bis(thiourea) derivatives were synthesized and their enantiomeric recognition abilities toward the enantiomers of tetrabutylammonium salts of α-hydroxy and N-protected α-amino acids were examined in acetonitrile using fluorescence spectroscopy.

Original languageEnglish
Pages (from-to)918-922
Number of pages5
JournalTetrahedron Asymmetry
Volume27
Issue number19
DOIs
Publication statusPublished - Oct 15 2016

Fingerprint

Thiourea
Enantiomers
Thioureas
enantiomers
thioureas
Fluorescence spectroscopy
Acetonitrile
ureas
Urea
acetonitrile
amino acids
Amino acids
Salts
salts
Derivatives
Amino Acids
fluorescence
synthesis
spectroscopy
tetrabutylammonium

ASJC Scopus subject areas

  • Catalysis
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

Cite this

Synthesis and enantiomeric recognition studies of optically active 5,5-dioxophenothiazine bis(urea) and bis(thiourea) derivatives. / Pál, Dávid; Móczár, Ildikó; Kormos, Attila; Baranyai, P.; Huszthy, P.

In: Tetrahedron Asymmetry, Vol. 27, No. 19, 15.10.2016, p. 918-922.

Research output: Contribution to journalArticle

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